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Computerized Risk Assessment in an Employee Population

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00153335
First Posted: September 12, 2005
Last Update Posted: February 26, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
University of New Mexico
Information provided by:
Centers for Disease Control and Prevention
  Purpose
This is a study to determine whether a computerized risk assessment and focused patient provider interaction can improve health outcomes in an employee population.

Condition Intervention
Healthy Behavioral: patient-provider interaction

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Official Title: Computerized Risk Assessment in an Employee Population

Further study details as provided by Centers for Disease Control and Prevention:

Primary Outcome Measures:
  • Satisfaction at time of visit
  • Utilization of health services at one year
  • Health outcome at one year

Secondary Outcome Measures:
  • Stage of change for health behaviors at one year
  • Quality of life at one year
  • Work performance at one year

Estimated Enrollment: 300
Study Start Date: June 2005
Study Completion Date: September 2007
Detailed Description:

The overall goal of the proposed research is to test the effectiveness of a theoretically-based interactive behavioral and health risk assessment system to improve the mental and physical health outcomes of the primary care provided for the adult multicultural members of a university health center-employee-based practice. The new system will include:

  1. administration of a computerized behavioral and health risk assessment,
  2. calculation of an individualized risk profile for each patient participant,
  3. individual patient computerized video training in interaction focused on the risk profile,
  4. physician training in patient-provider interaction, motivational interviewing and counseling, and in referral and triage focused on the risk profile, and
  5. development of a negotiated care plan between patient and clinician for follow-up care.

Expected outcomes include changes in: risk category scores, utilization patterns, costs for health care services, and health stage of change indicators. Expected impacts (mediating variables) are: compliance with recommendations, health locus of control, differences in patient-provider interaction patterns and patient and clinician satisfaction. If successful, this methodology would contribute significantly to the health promotion goals of Healthy People 2010 and provide much needed evidence of how a behavioral and health risk assessment system can help to reduce ethnic health disparities of multi-cultural populations. This proposal is responsive to CDC's RFA for Health Promotion in the Workplace; in particular it responds to requests for strategy #6: Identification and evaluation of public health informatics and communication strategies and tools to improve health decisions, health alerting, health literacy, or health assessment among employees and employer.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Employees who use University of New Mexico providers for medical care
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00153335


Locations
United States, New Mexico
University of New Mexico Health Sciences Center
Albuquerque, New Mexico, United States, 87131
Sponsors and Collaborators
Centers for Disease Control and Prevention
University of New Mexico
Investigators
Principal Investigator: Deborah L. Helitzer, ScD University of New Mexico
  More Information

ClinicalTrials.gov Identifier: NCT00153335     History of Changes
Other Study ID Numbers: CDC-OPHR-R01CD000122
R01CD000122 ( U.S. NIH Grant/Contract )
First Submitted: September 7, 2005
First Posted: September 12, 2005
Last Update Posted: February 26, 2010
Last Verified: February 2010

Keywords provided by Centers for Disease Control and Prevention:
Health Risk Assessment
Behavior Change
Patient-Provider Interaction
Employee Health
Absenteeism
Tobacco Use
Substance Use
Diet
Exercise
Medication Adherence